Multicentre randomised cotrolled trial comparing bipolar with monopolar transurethral resection of the prostate
Phase 3
- Conditions
- Benign prostatic hyperplasia
- Registration Number
- JPRN-UMIN000010801
- Lead Sponsor
- osaka medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Exclusion criteria were patients with documented or suspected prostate cancer, bladder calculus, neurogenic bladder, previous prostate surgery, renal impairment, associated hydronephrosis, and urethral stricture.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary end point in this study was safety, with a focus on perioperative findings such as operation time, decline of sodium level, clot retention, transfusion, and any other symptom relating to the procedures.
- Secondary Outcome Measures
Name Time Method Secondary endpoints were efficacy findings for patients after 36 months of follow-ups including development of urethral stricture.